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Advanced Imaging of Arthritis
Andrea S. Doria, MD, PhD, MSc
The Hospital for Sick Children
Toronto, Canada
May 15, 2013
Speaker disclosure
DISCLOSURES
DISCLOSURESFOR:
FOR: ANDREA
ANDREAS.
S.DORIA
DORIA
DISCLOSURES FOR: ANDREA S. DORIA
WFH requires the following disclosures be made at each presentation:
Conflict
Research Support
Disclosure - if conflict of interest exists
Baxter Inc (Research Grant), Bayer
Healthcare Inc (Research Grant), Pfizer
(Student Salary Support)
Director, Officer, Employee
Shareholder
Honoraria
ADDITIONAL
TEXT EXAMPLE
Advisory Committee
Consultant
Baxter Steering Committee
International Prophylaxis Study Group (not
for profit); Baxter Steering Committee
OUTLINE
CLINICAL IMAGING TOOLS
1. Available imaging modalities for early diagnosis - physics
characteristics of imaging modalities
2. What is currently available in clinical practice – Data Acquisition
and Interpretation
INVESTIGATIONAL IMAGING TOOLS
3. What can potentially be available in clinical practice in the
future - Laboratory to clinical translation
PHYSIOPATHOGENESIS - ARTHRITIS
Juvenile Idiopathic Arthritis
Hemophilic Arthritis
Trigger point:
antigen
(?autoimmune)
Trigger point: iron
(intraarticular
bleed)
reactive arthritis
vessels grow in an uncontrolled
and disorganized manner
vascular pannus
erodes the underlying cartilage
Anatomic Imaging Targets in Arthritis
Functional / Molecular Imaging Targets in Arthritis
Illustration of physiologic processes in inflammatory arthritis ranging from pre-lesional disfunction (left)
Illustration of physiologic processes in inflammatory arthritis ranging from pre-lesional disfunction (left)
through
recruitmenttoto
development
of angiogenesis
throughmonocyte
monocyte recruitment
thethe
development
of angiogenesis
(right). (right).
Inflammation
Hypoxia
Inflammation
Hypoxia
Angiogenesis
Angiogenesis
Adapted from Nature Reviews 2004; 3: 914
Adapted from Nature Reviews 2004; 3: 914
Choudhury RP, Fuster V, Fayad ZA. Nat Rev Drug Discov 2004;3:913-925
Question #1 – Arthritis Subtypes
Which are not subtypes of Juvenile Idiopathic Arthritis
(JIA)?
A. Enthesitis-related arthritis
B. Psoriasis
C.Oligoarthritis
D. Systemic arthritis
E. CRMO
Juvenile Idiopathic Arthritis
Classification of juvenile idiopathic arthritis (Durban, 1997)
Onset <16 years
Duration: 6 weeks
Subtypes:
1. Systemic arthritis
2. Oligoarthritis
Persistent
Extended
3. Polyarthritis (rheumatoid factor negative)
4. Polyarthritis (rheumatoid factor positive)
5. Psoriatic arthritis
6. Enthesitis-related arthritis
7. Other
Does not meet criteria for any of categories 1-6
Meets criteria for more than one of categories 1-6
X-Ray and CT
Physics Concept:
Differential absorption of low energy x-rays as they are
attenuated during their transmission through the body from
source to detector
Advantages:
-High spatial resolution
-CT development with multirow detector systems: improved
temporal resolution – potential for measurement of
physiologic perfusion rather than only morphologic
assessment
Disadvantages:
-Limited soft-tissue contrast sensitivity
-Deleterious x-ray energy absorption
Conventional Imaging
Advanced Imaging - Radiography
Talbot-Lau Interferometer - X-Ray Refraction of 1/10,000 of a Degree
Innovative x-ray device that produces image contrast from phase differences of the x-rays
that pass through the target with an ordinary x-ray source. Cartilage does not absorb many
x-rays and therefore, it is difficult to photograph. This device produces contrast by detecting
x-rays that have bent 1/10,000 degree (Talbot-Lau Interferometry). As a result, tissues that
otherwise could not be visualizable by x-rays can be captured.
http://sciencelinks.jp/content/view/1228/365/
Advanced Imaging - Perfusion CT
Increased number of detector arrays
Nonionic iodinated contrast agents
Fundamental basis for contrast
enhancement in CT: exchange of
small molecules, iodinated
contrast material, between the
intravascular space and the
extravascular interstitial space
after intravenous administration
of the contrast material.
Evaluation of organ
perfusion
Nuclear Isotope Imaging
Physics Concept:
X-rays: Differential transmission of external ionizing
radiation
Nuclear Medicine: Differential radioisotope uptake within a
particular organ system using radionuclides of different
emitted gamma energy
PET: radionuclides are positron emitters that
necessitate coincidence detection = improves contrast
to noise through better background suppression
Positron Emission Tomography (PET)
Advantages
1. Ability to spatially localize biologically relevant processes
2. Imaging Merging Technology: PET / CT = high spatial
resolution of CT + high specificity of PET radiotracers
Disadvantages
1. Short half-lives of positron-emitting radioisotopes: difficult
production and distribution (cyclotron interactions: 18F, 15O, 11C)
2. Possibility of following one molecular species in a given imaging
experiment
3. Limited CNR because of excessive absorption (radiation
exposure)
4. Tradeoff between spatial resolution (based on collimator designs)
and SNR = higher SNR with larger collimator aperture but decreased
spatial resolution
Positron Emission Tomography (PET)
Rabbit Model of Blood-Induced Arthritis
Shammas A, Doria AS et al. World Federation of Hemophilia, Buenos Aires, 2010
PET- MRI Fusion Imaging
- Complementary anatomic and molecular information. Since predicting remission is
important but currently limited to score-based methods and timing of treatment affects
Prognosis, dual MRI-PET may benefit patients with arthritis by providing a rapid and
detailed assessment of disease status and treatment response.
-Challenges: use of radioactive probes and high cost
Fusion of high-resolution 18F-FDG-PET with MRI for a rheumatoid arthritis therapy responder.
Jeffrey T, et al. Top Magn Reson Imaging 2011; 22: 61–69
Ultrasound
Physics Concept:
Differential reflection of sound waves as they travel through
tissue
Molecular imaging application: based on the use of contrast
agents (“bubbles”)
Conventional Imaging: Advantages of Ultrasound
for Evaluation of Arthritic Joints
• Relatively inexpensive imaging modality
• Easy access
• No requirement for sedation for imaging of joints of
children under the age of 7 years (as opposed to MRI)
•Color/power Doppler: potential for synovial vasculature
visualization without IV contrast administration
•Lack of susceptibility artifacts (“blooming”) from
extracellular hemosiderin deposition on gradient-echo
images
• Ability to differentiate effusion, synovium and hemosiderin
Ultrasound – Capability of Identification of Blood Products?
PD-weighted
+C T1-weighted
Cranial
b.
T2-weighted
c.
*
*
*
Caudal
e.
*
Cranial
f.
*
Caudal
*
Differentiation between effusion, synovium and hemosiderin
MRI:
sometimes
not possible
Hemosiderin
Fluid
US: clear
differentiation
Hemosiderin
Fluid
Synovium
Cartilage
Challenges of Ultrasound for Assessment of
Arthritis Joints
DATA ACQUISITION
-Operator-dependent – Experience is required
DATA INTERPRETATION
-Adjustment with MRI scales: suitable for assessment of
the whole joint (overall assessment), not only the edges
of the joints
-Quantification of diagnostic test sensitivity loss and
correlation with clinical significance
-Need for normative data for comparison of physiologic
and pathologic cartilage thinning (true for both US and
MRI)
Limited Field-of-View of Ultrasound Imaging
L2 Ant Sag Med
Cor T2
US “ sees” only the external
aspect of the articular surface
Limitations of Ultrasound Compared with MRI
Cartilage
Central portion cannot be visualized on US - most of the
osteochondral changes are seen at the periphery of the joint
Posterior aspect of patella cannot be visualized on US
Challenges on positioning of transducer (angle of ultrasound
beam)
IMAGING PROTOCOL FOR ULTRASOUND–Data Acquisition
L1- above the joint line
L2 – at the joint line
L3 – below the joint line
KNEES
ANT – Anterior, POST – Posterior, CEN – central, SAG
MED – between central and medial most
LAT - between central and lateral most
ANKLES
IMAGING PROTOCOL FOR ULTRASOUND–Data Acquisition
Transducer position in the sagittal plane for ultrasound scanning of knees and ankles.
Keshava et al.
Haemophilia
2009
CARTILAGE LOSS
L1 Ant Ax Med
L1 Ant Sag Lat
Sag PD
Ultrasound
Advances
Real-time 3D imaging
Ultrasound biomicroscopy
Tissue characterization with specifically designed contrast
agents
Question #2 – Advanced US Imaging
Which is not an advantage of 3DUS over conventional
2DUS imaging for assessment of arthritis?
A. Improved reliability and reproducibility in serial measurements
B. Electronically controlled transducers: less motion artifact with
the use of mechanical arms
C. Possibility of compression of images during scanning
Advanced Imaging: Advantages of 3DUS for
Evaluation of Arthritic Joints
-Images in different viewing planes can be reconstructed using 3D
data acquired, including the coronal plane which is not always
possible in 2D
-Improved reliability and reproducibility in serial measurements
Watanabe T, et al. Clin Rheumatol 2012; 31:299-307
Iagnocco A, et al. Rheumatology (Oxford) 2011; 50:1409-1413
-Superior visualization of the synovial space (compared to 2DUS)
including subtle changes in the microvasculature and morphology of
the synovial membrane and articular cartilage
- Electronically controlled transducers: 2DUS transducers are held and
controlled manually. 2DUS imaging requires that users mentally
integrate 2D images to form an impression of 3D structures
Advanced Imaging: Disadvantages of 3DUS
- Mismatches between the motorized linear scanning
mechanism and the irregular contour of the knee with loss
of contact during scanning
- Reconstruction into a single combined 3D image of the
knee requires co-registration of images: time consuming
-More cumbersome process: involves adding a
mechanical motor to the transducer and may be more
difficult for the user to manipulate.
-On 2DUS, the operator can compress the area being
imaged which is difficult to be implemented at 3DUS
-Using the motorized linear scanning mechanism, color
Doppler suffers from motion-related artifact,
Doppler 2DUS and 3DUS
indistinguishable from true signal
images in the
Possible solutions:
Use of a different position sensing mechanism such as a
magnetic-track probe or a curved scanning mechanism
suprapatellar bursa of a
JIA patient. Note the
Significant artifact due to
the motion from the
motarized mechanism.
3DUS Data Acquisition Techniques
• Free-hand scanning without position
sensing – 3D images are reconstructed on
the assumption that the operator is moving
the transducer in a smooth, steady motion
while capturing 2D images at regular
intervals in a linear or angular fashion highly user dependent
• Free-hand scanning with position sensing –
Uses a transducer with articulated arms
and magnetic field sensors to track the
position and orientation of the US probe .
• Two-dimensional array scanning for
dynamic three-dimensional US – Uses a
stationary 2D transducer array to generate
real-time 3D images.
• Mechanical scanning – Uses a motorized
mechanism to translate, tilt, or rotate a
conventional transducer to acquire a
sequential series of 2DUS images.
Setup for 3DUS
Hardware and software:
a. 3D hardware coupled with
the conventional
ultrasound transducer.
b. Enlarged view of motorized
mechanism attached to a
conventional 2DUS
transducer used to
translate the transducer
and capture a linear series
of 2DUS images
c.
3DUS software (Wing) that
enables real-time images
to be visualized in 3D
during scanning
b.
a.
c.
2DUS images & 3DUS images
Sagittal 3DUS (a) and 2DUS
(b) images of the suprapatellar
pouch with joint effusion, and
axial 3DUS (c) and 2DUS (d)
images of the distal femur in a
patient with JIA
a.
b.
c.
d.
3D reconstructions allow users
to have a better appreciation
for the 3D anatomy (i.e.,
cartilage volume)
Images can be reproduced in
any plane – as in a virtual
patient
3DUS-MR Fusion Imaging
• Definition: superposition of US and MRI
images
• Potential advantages of 3DUS-MR fusion
imaging:
– Allows users to merge real-time US
images with retrospective MR images,
which can improve US operator
confidence, as well as anatomical and
functional correlations
– Provides MRI reference points as
anatomic landmarks in serial US
examinations, which may improve
reproducibility in disease follow-up and
therapy monitoring
• Disadvantages: extra cost and time
associated with its use
Sagittal T1-weighted MR image
of the knee with a joint effusion
with ROI (green) corresponding
to a sagittal 3DUS image at the
level of L0 central.
Ultrasound Biomicroscopy
#669 rt med
CARTILAGE
Lesion not seen macroscopically
11 mm
= 11000
11 mm
= 11000
m m
Doria et al. Pediatr Radiol 2004
Ultrasound Biomicroscopy
CARTILAGE
Normal
11 mm
A.
Lesion not seen
macroscopically
Lesion seen macroscopically
B.
C.
Doria et al. Pediatr Radiol 2004
Ultrasound
Contrast-Enhanced Ultrasound
Principles for Use in Molecular Imaging:
1. If the wavelength of the transducer is matched to the
properties of a given contrast agent bubble, a specific
signature can be measured
2. The US probes receive signals based on the collapse
of the bubble during US scanning
SOFT TISSUES
Contrast-Enhanced Ultrasound - Humans
Doria et al. Pediatr Radiol 2001; 31: 524-531
Contrast-Enhanced Ultrasound
Rabbit Model of Inflammatory Arthritis
Microbubble destruction-reperfusion technique:
• measures the regional blood flow and vascular volume
0.5 sec
1 sec
AA
2 sec
5 sec
10 sec
20 sec
30 sec
R (T) = a (1 – e-bt)
Ab
• (b) a mean velocity
• Initial slope a flow rate
• Asymptote (A) a vascular volume
Doria et al. Pediatr Radiol 2006; 36: 1242–1251
Contrast-Enhanced Ultrasound
Rabbit Model of Inflammatory Arthritis (Antigen: Albumin)
Flow rate
Day 1 of arthritis
Mean velocity
Day 14 of arthritis
Doria et al. Pediatr Radiol 2006; 36: 1242–1251
Optical Imaging
Physics Concept:
Light microscopy is the primary tool for biologic imaging at
the cellular level
Advantages:
High temporal resolution
Good SNR
Disadvantages:
Molecular level
Small depth of tissue penetration, which is limited by
absorption and scattering of light
Optical Imaging
BIOLUMINESCENCE
Principle: occurs when the energy is supplied by a
biochemical reaction
Biswal S. Arthritis in Color. Saunders, 2009
Optical Imaging
PHOTOACOUSTIC IMAGING (PAI)
Principle: a short-pulsed laser is
used to illuminate the tissue
sample and generate
photoacoustic waves due to the
transient thermoelastic
expansion in the tissue. PAI is
highly sensitive to molecular
conformation of biological
tissues and can aid in describing
tissue functional hemodynamic
changes such as angiogenesis
and hypoxia in pathologic
synovium, providing imaging at
cellular and molecular levels.
Chamberland D et al. Integr Biol (Camb) 2010; 2:496-509
MRI
Physics Concept:
Interrogation of tissue water protons through the differential
population of proton spins
Limitations:
Resolution and SNR are dependent on gradient strengths,
radiofrequency RF coils and main magnetic field strength
Use of MRI in functional imaging:
Indirect detection mode by watching the influence on tissue
relaxations resulting from sequence parameters designed
to capture signal at specific points in the relaxation curve
(e.g. BOLD) or with the use of contrast agents (e.g.
gadolinium, iron oxide)
Question #3 – Advanced MR Imaging
Which is an MRI technique that estimates of the physiologic
properties of the synovial microvessels in JIA, including
blood/plasma volume, and transendothelial permeability of
the contrast agent?
A. MR Spectroscopy
B. Dynamic MRI (positive contrast agent: gadolinium)
C. Blood oxygen level dependent (BOLD)
D. MRI (negative contrast agent: ultrasmall paramagnetic
iron oxide [USPIO])
E. Diffusion-weighted imaging
Conventional MRI
Synovitis
• T1/PD
• Gadolinium
Sag T1
Ax T1 fat sat
Conventional MRI
Osteochondral Abnormalities
• Cartilage loss
• Erosions
• Subchondral
cysts
Sag T2
Cor T1
Today’s Imaging
HIGH-END CLINICALLY AVAILABLE MRI TECHNIQUES
Data Acquisition
1.5 vs 3 Tesla MRI Scanners
3D SPGR
FS SSFP
Dixon
1.5 T
3T
Kornaat et al. Osteoarthritis Cartilage 2005; 13: 338-344
High Resolution Coils
PARALLEL MRI
ASSET PD
Gradient-echo
75% reduction
in scanning
time using
parallel imaging
rather than
conventional
imaging
ASSET T2
Protocol for ERA:
Cor STIR Multistation
(scan time: 28 min)
Sag STIR Spine
Ax obl STIR SI joints
Cor obl STIR SI joints
Sag STIR Knees
Sag STIR Ankles
(scan time: 30 min)
Scan time: 58 min
Body coil
WHOLE BODY MRI
Not
involved
MRI SEGMENTATION – QUANTITATIVE ASSESSMENT OF CARTILAGE
Results of this study: The
semi-quantitative method is
A
valid post.
for assessment
of
1 Schicht
Bull
Bull
eye
Rat
Test
2D
MT
Rat
Test
2D LT
pathologic
cartilage
status
in
eye
Lateral
Osteophyt
cross-sectional
studies of Rat Test 2D LT
blood-induced arthropathy in
ankles, however the
quantitative method is
suboptimal or less powerful
for this purpose.
The cartilage thickness
(ThCtAB) in the talar trochlea
measured 1.22 units and in
the distal tibia, 1.05 units.
Doria et al. Quantitative versus SemiQuantitative MR Imaging of Cartilage
in Blood-Induced Arthritic Ankles.
Preliminary Findings. SPR 2012.
C
B
D
FUNCTIONAL / MOLECULAR MRI TECHNIQUES
Today’s / Tomorrow’s Imaging
Matching of MRI sequences to tissue of interest
Tissue
Measurement
MRI sequence / technique
Synovium
Fluid
T2-weighted fast spin-echo MRI
Rate of transfer of contrast between
Dynamic contrast-enhanced MRI
plasma and extravascular
extracellular space
Restricted water motion
Diffusion tensor imaging
(inflammation proxy)
Cartilage
Cartilage hydration and collagen
T2-mapping MRI
orientation
Bone
Glycosaminoglycan content
Delayed gadolinium enhanced MRI
Proteoglycan depletion
23Na MRI
Proteoglycan content
T1 rho MRI
Erosions
T1-weighted MRI
Bone marrow edema
T2-weighted fast spin-echo or short tau
inversion recovery (STIR) MRI
SYNOVIUM
BOLD MRI
Basal State
Oxy-Hb
Deoxy-Hb
Oxy-Hb
Activated State
Deoxy-Hb
Changes in Blood Oxygenation level cause changes in MR Decay of T2*
BOLD MRI - Rationale
Inflammation
Oxygenation
ANGIOGENESIS
Oxygenation
Metabolic demand
Vascular system of the knee
Synovial cell
Artery
O2 consumption
ACUTE ARTHRITIS
(day 1)
BOLD signal intensity decreases /
increases reflecting decrease in venous
pO2 (increased oxygen extraction) or
synovial hyperemia
Hypothesis
Negative correlation:
BOLD = synovial
hyperemia
BOLD signal
on-and-off
differences
Arthritic knees
pO2 vein
Vein
CHRONIC ARTHRITIS
(day 28)
BOLD signal intensity
returns to baseline values
Alternative
Positive correlation
BOLD = oxygen
extraction
BOLD signal Arthritic knees
on-and-off
differences
pO2 vein
0
1
28 Timepoints
0
1
28 Timepoints
BOLD MRI
Application in Inflammatory Arthritis in a Rabbit Model. Antigen: Carrageenin
BOLD MRI is feasible to depict synovial changes during progression of
experimental arthritis. We did not define the biological basis for the BOLD MRI
changes noted over time since histologic assessment did not explain the
physiologic events of the experiment. Required further validation of the technique
A
AI
B
a
.
day 0
day 28
day
0
C
A
I
b
.
AI
BOLD Signal
Intensity (a.u.)
day 1
day 0
A
dayB
28
day 1
day 28
C
F
E
SI
SI
H
G
NI
c.
I
d
.
NI
BOLD Signal
Intensity (a.u.)
D
D
G
E
F
BOLD Signal
Intensity (a.u.)
Timeframes
G
H
I
Doria et al. Acad Radiol 2005
BOLD MRI
Acad Radiol 2005; 12: 841-852
Acad Radiol 2011; 18: 615-626
Diff on_off _.01_ Pos_Neg
BOLD MRI
Hypothesis
Positive correlation:
BOLD = oxygen extraction
P = .0001
Intraarticular pO2 concentration
BOLD signal
on-and-off
differences
Arthritic knees
pO2 vein
0
1
28 Timepoints
Doria et al. Radiology
2007
P < .05
BOLD imaging correlated moderately (r = .54, P < .0001) with knee diameters, and
weakly (r = .35, P = .01) with laboratory indices (high threshold for analysis)
Translation to Humans (JIA Patients) at 1.5 Tesla
Day 45
CONTROL
KNEE
CONTRALATERAL
KNEE
PATHOLOGIC
KNEE
Day 0
Results of this study show that numerically BOLD
MRI values were greater in knees with active
inflammation than in contralateral unaffected knees,
and interval pre- and post-injection changes were
greater in the arthritic group than in the group of
contralateral joints.
Doria A.S., Crawley A., Babyn P., Rayner T., Feldman B. BOLD MRI at 1.5 Tesla in
Huppertz
et al. In
J Pediatr
Juvenile Idiopathic Arthritis: Preliminary Experience.
Clinics 2013
Press 1995
Translation to Humans (JIA Patients) at 3.0 Tesla
JIA patient – Bilateral knee involvement, right worse
CO2 Challenge
b.
Asymptomatic Contralateral Knee
a. Juvenile Idiopathic Arthritis Knee
b.
Asymptomatic Contralateral Knee
Percentage (%) BOLD signal change
a. Pathologic: median [SD], 1.27 [0.84])
b. Asymptomatic: median [SD], -0.31 [0.08]
c. Control Healthy Knee
c. Median [SD], 0.12 [0.32])
Translation to Humans (JIA Patients) at 3.0 Tesla
Expected BOLD signal in arthritic, aysmptomatic contralateral and
healthy joints and coxyhemoglobin/deoxyhemoglobin ratios
Maximum values
Ratios
Oxyhemoglobin
BOLD signal
Healthy joint
Deoxyhemoglobin
Asymptomatic
(in remission) joint
Oxyhemoglobin
Deoxyhemoglobin
Arthritic joint
Oxyhemoglobin
Deoxyhemoglobin
Minimum values
DCE MRI
SYNOVIUM
DCE MRI of the inflamed synovium: provides estimates of the
physiologic properties of the synovial microvessels, including
blood/plasma volume, and transendothelial permeability of
the contrast agent
Gd-DTPA: Microvascular agent
Parameters:
-Time-to-peak (TTP)
Results in this study:
In arthritic knees increased capillary
permeability is expected to take pl
ace in early disease as compared with
baseline, mid-term (day 14 of arthritis) and
late disease (day 28 of arthritis)
measurements.
-Signal enhancement
-Peak enhancement
Doria et al. AJR 2006; 186: 1165-1171
Dynamic Contrast-Enhanced MRI: In vivo capillary permeability and signal
slope have distinctive dynamic MRI properties. The accuracy of MRI parameters for
diagnostic evaluation of experimental arthritis differs according to the stage of disease
Day 0 of arthritis
Day 1 of arthritis
Day 1 of arthritis
Difference of AUCs: time-to-peak (TTP) and other
parameters on day 1, P = 0.0002 and signal slope (dS/dt),
capillary permeability (kPSr) and other parameters on day
14, P = 0.001
Day 14 of arthritis
Doria et al. AJR 2006
Ultrasmall Superparamagnetic Iron-Oxide Contrast Agents
(USPIO) MRI
SYNOVIUM
Biswal S. Arthritis in Color. Saunders, 2009
Ultrasmall Superparamagnetic Iron-Oxide Contrast Agents
(USPIO) MRI
Rabbit Model of Blood-Induced Arthritis
Pre-contrast
A.
Post-contrast
(48 hr after injection)
B.
NEGATIVE
contrast
agent
Amirabadi, Doria et al. World Federation of Hemophilia, Buenos Aires, 2010
Delayed Gadolinium-DTPA-Enhanced T1 Mapping MRI (dGEMRIC)
CARTILAGE
- Sensitive to cartilage proteoglycan content
Due to negatively charged glycosaminoglycans (GAG) sidechains,
proteoglycans attract cations and water into the tissue, causing a swelling
pressure
T1 relaxation time in presence of the contrast agent is linearly related to the
GAG content
Bashir et al. Radiology 1997
Biswal S. Arthritis in Color. Saunders, 2009
T1 rho MRI
CARTILAGE
Able to detect early intracartilaginous degeneration quantitatively and also
qualitatively by color mapping demonstrating a higher sensitivity than standard
T2-weighted sequences. The results of this technique highly correlate with
reduced proteoglycan content and disrupted collagen architecture as measured
by biochemistry and histology
Area of
inhomogeneity
Jobke B, Bolbos R, Saadat E, et al. MRI 2013; 31: 156-161
T2 Mapping MRI
CARTILAGE
T2 measurements may characterize the structural integrity of the cartilaginous tissue
and quantitatively assess the degree of cartilaginous degeneration (proteoglycans)
Spatial variation of T2 correlates with the 3D arrangement of the collagen fibrils
Potential: detection of proteoglycans changes prior to anatomic damage
A.
B.
Dardzinski et al. Radiology 2002
T2 Mapping
MRI
HEMOPHILIC
ARTHROPATHY
CARTILAGE
Rabbit Model of Blood-Induced Arthritis
Overall decrease in average T2 values in
arthritic knees over time regardless of the use
or not of USPIO contrast agent (P<0.0001)
Amirabadi, Doria et al. ISMRM 2009
T2 Mapping of Cartilage – Picrosirus Staining
Baseline - Medial
Week 10 - Medial
Diffusion-Weighted MRI
CARTILAGE / BONE
- Demonstrates the normal translational movement (Brownian
motion) of water molecules that occurs in all tissues
- Alteration of normal diffusion can occur in pathological events
with a loss of tissue integrity. This technique is promising for
evaluating ischemic tissues, and functional changes associated
with osteoporosis.
MacKenzie, Jaramillo et al. Pediatr Radiol 2007; 37: 781-788
Diffusion Tensor Imaging (DTI)
CARTILAGE
- Characterizes the in vivo 3D
arrangements of collagen fibres
- Allows determination of the directionality
as well as the magnitude, form, trend and
integrity of a particular anatomic region
[Govoni et al 2004].
The highly ordered structure of the collagen
matrix is induces anisotropy in the diffusivity
of water, so that measuring the anisotropy of
diffusion could give direct information on the
integrity of the collagen matrix. Also, DTI
may be sensitive to the proteoglycan (PG)
content through mean diffusivity . Therefore,
it is a promising technique for the diagnostic
workup of articular cartilage, especially since
it may be sensitive to both PG content and
collagen fiber architecture.
Raya JG, Melkus G, Adam-Neumair S, et al. Radiology 2013; 266: 831-841
MicroMRI
BONE
- Acquires images at a resolution sufficient to visualize individual bony
trabeculae and to obtain quantitative information in the form of structural
parameters similar to those of histomorphometry
The in-plane image resolution with this technique is approximately 156
micrometers which is similar to the dimensions of the bony trabeculae (78-200
micrometers)
Wehrli et al. Radiology 1998
MRI Spectroscopy
Physics Concept:
Detects protons on a molecule which have a unique
signature that can be discerned in an MR spectroscopy
experiment
Disadvantages:
Low SNR
MRI Spectroscopy - METABONOMICS
SYNOVIUM FLUID
Principle: 1H NMR spectroscopic analysis of biofluids enables the
generation of spectral profiles of a wide range of low molecular
weight metabolites that reflect the metabolic status of an
organism.
Perturbation of the homeostatic system of an organism by drug-induced toxicity
or disease initiates a metabolic change detectable in the spectral profile.
The Problem: With advancement of MRS technology: visual
analysis was not the optimal way to interpret biofluid spectra (too
complex).
Metabonomics: Systems approach to investigating the metabolic
consequences of (patho)physiological or genetic modification in a
multivariate and dynamic manner. Enables interpreting large
databases of 1H NMR urine and plasma spectra in various states of
health and disease.
Holmes & Antti. Analyst 2002; 127: 1549-1557
MRI Spectroscopy - METABONOMICS
Multivariate Statistical Analysis of 1H NMR spectra:
Searching for patterns in the NMR spectral profile
Strategy of metabonomic ‘expert system’
Stackplot of 600 MHz 1H NMR spectra of
for toxicity screening
urine obtained from rats treated with
tissuespecific toxins
Holmes & Antti. Analyst 2002; 127: 1549-1557
Hyperpolarized MRI
Purpose: Polarization of metabolically active substrates such as pyruvate permits in vivo
metabolic imaging of the injected agent and downstream metabolic products. The metabolic
products can be differentiated from the substrate on the basis of their
chemical shifts.
Pyruvate levels are elevated in joints affected by osteoarthritis, and the amount of lactic
acid, a metabolic product of pyruvate, is elevated in the synovial fluid of patients with
rheumatoid arthritis.
Advantages:
-increased sensitivity in the
13C MRS experiment by
10,000-fold or more
- detection of 13C-labeled
substrates in vivo plus imaging
of their tissue
distribution
- Absence of background
signal from nonpolarized
material
MacKenzie JD, et al. Radiology 2011; 259(2): 414-420
Jeffrey T, et al. Top Magn Reson Imaging 2011; 22(2): 61–69
MRI
Clinically available
Investigational
Hardware
- High strength field MRI:
1.5 and 3 Tesla scanners
- High resolution coils
Software
- Parallel imaging: faster
scanning
- 3D Reconstruction
Synovium:
DCE MRI,
USPIO,
BOLD
Cartilage:
T2
mapping
Bone: osteoporosis - MicroMRI
The Future
Integrative Systems Approach to:
- Disease Diagnosis
- Treatment
- Monitoring
Intuition becomes
increasingly valuable
in the new information
society precisely
because there is so
much data.
John Naisbitt 1929-